Additional file 1 Table 1: Studies excluded from the systematic review Reference Aapro M. D et al. Seminars in Oncology 1998;25(5 SUPPL. 12):7-11. Abu-Khalaf MM et al.Breast Cancer Research and Treatment 2007;104(3):341-349. Abu-Khalaf MM, et al.Oncology 2005;69(5):372-383. Aisner J WV, et al. J Clin Oncol, Issn: 0732 183x. 1987;5(10):15231533. Akpek G, et al. Cancer 1368;86(7):1368-1376. Al Ismail SA, et al. European journal of cancer & clinical oncology 1987;23(9):1379-84. Alba E, et al. Breast Cancer Research and Treatment 2003;77(1):1-8. Alberts DS, et al. Drugs 1997;54(SUPPL. 4):30-35. Alberts DS, et al. Oncology 1997;11(10 SUPPL. 11):54-62. Alberts DS, et al. Seminars in Oncology 2004;31(SUPPL. 13):53-90. Aleman BMP, et al. Blood 1878;109(5):1878-1886. Allegra JC, et al. Investigational New Drugs 1985;3(2):153-61. Alliot CE. et al.. Journal of Clinical Oncology 2005;23(21):4797-4799. Amadori D, et al. Breast Cancer Research and Treatment 1998;49(3):209-217. Amat S, et al. 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Reason for exclusion Preliminary findings Evaluates paclitaxel Not RCT Cumulative dose not reported and response different between groups Not RCT Numbers randomized not reported Not RCT Not primary study Review Review Cohort study Dose received not reported No relevant comparison group No relevant comparison group Evaluates docetaxel Control group recruitment closed due to safety issues Tamoxifen Not RCT Cohort study Different doses epirubicin evaluated Different doses epirubicin based schedules evaluated Preliminary results Dose received not reported, response different in the two groups Evaluates tamoxifen Review Different doses compred Evaluates addition of radiotherapy Review High versus low dose Not RCT No anthracycline group Evaluates dose escalation Review Does not report treatment received Duplicate of Aviles 1994 included Weekly versus cyclical therapy Secondary report of RCT, no cardiotoxicity outcomes Standard dose versus dose dense therapy Evaluates paclitaxel Evaluates paclitaxel No non-doxorubicin arm Not RCT Dose intense versus standard dose Dose response Duplicate Swain 1997 – pharmacoeconomic analysis Not all patients randomised, not all on anthracyclines, no cardiac outcomes No appropriate control group Interim results, no numbers reported for cardiotiotoxicity, may be Bennet 1988 Review No non-anthracycline arm No cardiac outcomes Consensus treatment guidelines Insufficient data reported on cardiotoxicity as not prospectively collected Unavailable from British Library 1 Additional file 1 Reference Biganzoli L, et al. 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Carde P, et al. Journal of Clinical Oncology 1993;11(11):2258-72. Cardinale D,. Circulation 2006;114(23):2474-81. Carrio I, et al. J Nucl Med 1993;34(9):1503-7. Carmo-Pereira J, et al. British Journal of Cancer 1987;56(4):471-3. Carotenuto M et al. Leuk Lymphoma 1992;7(Suppl. 2):25-28. Casper ES. et al. Clin Trials J 1987;24(Suppl. 1):57-67. Casper ES. et al. Clin. Trials J. 1987;24(Suppl. 1):139-141. Cassier PA,. et al. Breast Cancer Research and Treatment 2008;109(2):343-350. Chan S, et al. Journal of Clinical Oncology 1999;17(8):2341-54. Chan Sm. et al. Oncology 1997;11(8 Suppl 8):19-24. Chang Ae. et al. Journal of clinical oncology : 1988;6(9):1491-500. Chang P et al. Procamerasscancer Res 1975;16(66):No.326. Colozza M, et al. European Journal of Cancer 2002;38(17):2279-2288. Cottin Y, et al. Clinical Cardiology 1998;21(9):665-670. Cowan JD,. et al. Investigational New Drugs 1985;3(2):149-52. Cresta S, et al. Annals of Oncology 2004;15(3):433-9. Dando TM,. et al. American Journal of Cancer 2005;4(3):193-206. De Lena M et al. Clinical Trials Journal 1987;24(Suppl 1):223-229. De Lena M, et al. Medical Oncology & Tumor Pharmacotherapy 1989;6(2):163-9. Di Trolio R, et al. International Journal of Immunopathology and Pharmacology 2006;19(2):253-263. Dogliotti L, et al. Journal of Clinical Oncology 1165;14(4):1165-1172. Dranitsaris G, et al.. Breast Cancer Research and Treatment 2008;107(3):443-450. Duchateau Pharmaceutisch Weekblad 1155;134(33):1155-1158. Reason for exclusion Retrospective analysis looking at age as a predictor of outcome Evaluates paclitaxel High versus standard dose No appropriate control arm Evaluates tamoxifen Secondary report Cumulative dose not reported Dose response study Dose response study, long term follow-up, observational Evaluates paclitaxel Dose response Evaluates docetaxel Evaluates docetaxel Patients crossover treatment groups if indicated and cardiotoxicity reported for both treatment periods combined Systematic Review No anthracycline group High dose versus low dose Preliminary results Systematic review Systematic review Does not report treatment recieved No appropriate comparison group CHOP versus CIOP, inferior efficacy, RCT terminated early Clinical trial, not randomised, baseline imbalances in prior chemo- and radiotherapy Evaluates addition of alpha interferon Evaluates paclitaxel Evaluates paclitaxel Evaluates one dosing stategy versus another Protocol for systematic review Review Evaluates paclitaxel Time intense therapy versus standard therapy No appropriate comparison group Not all patients on anthracyclines – mix of chemotherapy regimens Not RCT Two doses compared Preliminary results Duplicate of Casper 1987b Insufficient information on doses received Docetaxel versus paclitaxel Evaluates docetaxel Evaluates docetaxel High versus low dose No appropriate control group Tamoxifen also given Not RCT Interim results of an RCT Evaluates docetaxel Review Cardiac outcomes not reported fully Duplicate De Lena 1987 Systematic review No appropriate non anthracycline group Models risk from O’Brien RCT Secondary report of a study 2 Additional file 1 Reference Ec van Dalen et al. Cochrane Database of Systematic Reviews: Protocols 2007 Issue 3 John Wiley & Sons, Ltd Chichester, UK DOI: 10.1002/14651858.CD006647 2007(3). Ejlertsen B, et al. European Journal of Cancer 2007;43(5):877-84. el Mawla Ng. et al. Anti cancer drugs 1991;2(4):371-4. Engert A, et al.. Journal of Clinical Oncology 2007;25(23):3495-3502. Erkisi M, et al. Journal of Chemotherapy 1997;9(6):442-445. Fenk R,. et al. British Journal of Haematology 2005;130(4):588-594. Frasci G, et al. Oncology 2005;68(4-6):391-397. French Adjuvant Study Group. Journal of Clinical Oncology 2001;19(3):602-11. Frei BL, et al. Soefje SAE.. Journal of Pharmacy Practice 2008;21(2):146-158. Fumoleau P, et al.. Journal of Clinical Oncology 2003;21(6):1190-1191. Fumoleau P, et al. Drugs 1993;2:38-45. Fumoleau P et al. Proceedings of the American Society of Clinical Oncology 2001;20(Pt 1):28a. Fumoleau P, et al. l. Journal of Clinical Oncology 2003;21(2):298-305. Galetta F, et al. Biomedicine & Pharmacotherapy 2005;59(10):541-4. Ganz Pa et al. Journal of clinical oncology : 2008;26(8):1223-30. Gianni AM, et al. New England Journal of Medicine 1290;336(18):12901297. Giordano SH, et al.. Journal of the National Cancer Institute 2007;99(5):340-341. Giordano SH, et al. Journal of the National Cancer Institute 2008;100(4):230-231. Gill PS, et al.. Journal of Clinical Oncology 1996;14(8):2353-64. Glenn J, et al. Cancer 1206;55(6):1206-14. Glenn J, et al. Surgery 1985;97(3):316-25. Gregory RK, et al. European Journal of Cancer 2000;36(4):503-507. Guglielmi C, et al.. Haematologica 1989;74(6):563-9. Hamberg P, et al.. European Journal of Cancer 1514;43(10):1514-1528. Hardenbergh PH, et al. International Journal of Radiation Oncology, Biology, Physics 1999;45(1):69-72. Hasan SP, et al. Journal of the National Medical Association 2004;96(2 SUPPL):196-199. Healey Bird BRJ, et al. Clinical Cancer Research 2008;14(1):14-24. Heidemann E, et al. Onkologie 1990;13(1):24-7. Hequet O, et al. Journal of Clinical Oncology 1864;22(10):1864-1871. Iarussi D,. et al. Molecular Aspects of Medicine 1994;15(12). Iscoe N,. et al. Current Oncology 2003;10(1):27-35. Jensen BV. et al. Seminars in Oncology 2006;33(SUPPL. 8):15-21. Jurcut R, et al. Supportive Care in Cancer 2008;16(5):437-445. Keiling R, et al. Onkologie 1986;9 Suppl 1:8-10. Kinoshita T, et al.. International Journal of Hematology 2004;80(4):341350. Kleeberg URE. et al. Gynakologische Praxis 2008;32(1):134-136. Knight E et al. Procamerasscancer Res 1975;16(66):No.766. Kremer L C et al. Annals of Oncology 2002;13(6):819-829. Krupicka J, et al.. Leukemia & Lymphoma 2002;43(12):2325-9. Leonard Rc et al. Journal of clinical oncology : 1987;5(7):1056-63. Linden HM, et al. Journal of Clinical Oncology 2007;25(6):656-661. Lipshultz SE, et al. Heart 2008;94(4):525-533. Lopez M, et al.. Cancer 1989;64(12):2431-6. Macioch T, et al. Family Medicine and Primary Care Review 2006;8(3):997-999. Lopez M,. Oncology 1989;46(1):1-5. Magnus B et al., European Journal of Haematology 2008;80(6):477482. Mano M,. et al. Breast Cancer Research and Treatment 2005;89(1):8190. Martoni A, et al. Oncology 1990;47(5):427-32. Massidda B, et al. Anticancer Research 1997;17(1B):663-8. Maung K, et al. Clinical Breast Cancer 2002;3(3):183-184. Mellqvist UH, et al. Cancer 2008;112(1):129-135. Merli F, et al. Leukemia and Lymphoma 2007;48(2):367-373. Meyer RM, et al. Journal of Clinical Oncology 1995;13(9):2386-93. Reason for exclusion Systematic review Not received from British Library Dose comparison study Evaluates addition of chemo to radiotherapy Treatment received in each group unclear Dose comparison study Evaluates docetaxel Dose comparison study Review Letter Dose comparison study Evaluates docetaxel Dose comparison study Insufficient data for cardiac outcomes Long term follow up of selected patients from RCTs, observational study Dose comparison study Editorial Editorial Kaposi’s sarcoma Cardiotoxicity for RCT and non-RCT patients combined Cardiotoxicity for RCT and non-RCT patients combined Not RCT Duplicate study of 145 Review Chemotherapy and radiotherapy Retrospective analysis Review Duplicate Heidemann 1993 Not RCT Acute lymphoblastic leukemia Kaposi’s sarcoma Editorial – no primary data Review Duplicate FESG 1988 Dose comparison study Review Dose comparison study Systematic review Before and after comparison in participants from RCTs Cross over study, no useable outcomes Sequential versus simultaneous dosing Not primary study, narrative review Dose received not reported, difference in response Systematic review Duplicate of IMBSWE 1988 Meta-analysis Review Cross overs and dose received not clear Cardiac function not defined Secondary report of RCT Not an appropriate comparison group No appropriate comparison group Weekly versus standard dosing 3 Additional file 1 Reference Mori M, et al.. International Journal of Hematology 2005;81(3):246-54. Michelotti A, et al. Breast Cancer Research & Treatment 2000;59(2):133-9. Mori M, et al. Leukemia and Lymphoma 2001;41(3-4):359-366. Moser EC, et al. N Clinical Lymphoma & Myeloma 2005;6(2):122-30. Mouridsen HT, et al. Eur J Cancer Clin Oncol 1987;23(10):1477-83. Murphy CA, et al. Drug Safety 2007;30(9):783-804. Muss HB, et al. Cancer 1982;50(11):2269-74. Nair R, et al. Cancer 1998;82(11):2282-8. Nakamae H,. et al. Cancer 2005;104(11):2492-8. Namer M et al. European journal of cancer (Oxford, England : 1990) 2001;37(9):1132-40. Neidhart JA, et al. Journal of Clinical Oncology 1986;4(5):672-7. Neidhart JA, et al. Cancer Treatment Reviews 1983;10:41-6. Neidhart JA, et al. Seminars in Oncology 1984;11(3 Suppl 1):11-4. Nemoto T, et al. Cancer 1978;41(6):2073-7. Nielsen D, et al. Cancer Chemotherapy & Pharmacology 2000;46(6):459-66. Nielsen OS, et al. British Journal of Cancer 1998;78(12):1634-9. Nielsen OS, et al. 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Tebbi CK,et al. Journal of Clinical Oncology 2007;25(5):493-500. Tirelli U,. et al. Critical Reviews in Oncology/Hematology 2001;37(2):153-158. Reason for exclusion No appropriate comparison group Duplicate Venturini 1996 Not RCT Not RCT No cardiotoxicity outcomes Review No appropriate comparison group Treatment received unclear Not an RCT No appropriate comparison group Patients crossover treatment groups if indicated and cardiotoxicity reported for both treatment periods combined Patients crossover treatment groups if indicated and cardiotoxicity reported for both treatment periods combined Preliminary results of Niedhart 1986 No appropriate comparison group No appropriate comparison group High dose regimen Duplicate of Nielsen 1998 No cardiac outcomes reported Not RCT No cardiac outcomes No cardiac outcomes, just reports that they were ‘rare’ No cardiotoxicity outcomes No appropriate control group Before and after comparison, no non anthracycline comparison No appropriate control group No useable data for cardiotoxicity, gives mean treatment received in those with cardiotoxicity, not number of patients Dose comparison study Guidelines Evaluates paclitaxel No cardiac outcomes Evaluates paclitaxel No cardiac outcomes Not RCT Evaluates docetaxel Duplicate Swain 1997 No appropriate comparison group No appropriate comparison group Cardiotoxicity not an outcome Russian Duplicate Speyer 1992, no additional data Duplicate Speyer 1992, no additional data Editorial Preliminary results Long term followup of participants in RCT but not all patients Observational study No appropriate control arm – one dose versus another Japanese language Unclear if randomised No cardiac outcomes Review 4 Additional file 1 Reference Tirelli U, et al. Journal of Clinical Oncology 1998;16(1):27-34. Torti FM, et al. Ann Intern Med 1983;99(6):745-9. Tranum Bl 1982;49(5):835-839. Tsimberidou AM, et al. Blood 2002;100(13):4351-4357. Tsurumi H, et al. Journal of Cancer Research and Clinical Oncology 2004;130(2):107-113. Unverferth DV, et al. Semin Oncol 1983;10(1 Suppl 1):49-52. Uthayakumar S, et al. Aids 1996;10(5):515-9. Van Dalen EC, et al. Cochrane Database of Systematic Reviews 2006;4. Van Toorn DW, et al. Breast Cancer Research and Treatment 2000;60(1):57-62. Ventura GJE. et al. Journal of Clinical Oncology 2005;23(12). Verdonck LF, et al. Blood 2007;109(7):2759-2766. Vici P,. Clinica Terapeutica 1998;149(921):15-20. Weisberg SR et al. Proceedings of ASCO 1992;;Vol. 11:91. Wilson Re. et al. Archives of surgery (Chicago, Ill. : 1960) 1986;121(11):1354-9. Wolff AC, et al. Surgical Oncology 1999;8(2):93-101. Reason for exclusion No appropriate comparison group Not an RCT No appropriate comparison group No cardiac outcomes Treatment received not clear, difference in response No cardiac outcomes Kaposi’s sarcoma Systematic review Dose comparison study Letter – no primary data Dose comparison study Duplicate Lopex 1998 Duplicate Swain 1997 Does not report treatment received Review 5